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The role involves monitoring clinical trial sites, ensuring protocol adherence, reporting serious adverse events, and training new staff, with 5+ years' experience required.

Responsible for monitoring clinical trials, ensuring compliance with protocols, data integrity, site management, and training new employees, with significant oncology experience required.

The Sr. CRA 2 will monitor clinical trial sites, manage study compliance, ensure data integrity, and oversee patient safety in oncology studies, requiring strong clinical judgment and teamwork.

The Sr. CRA 2 will monitor clinical trials, manage study sites, ensure regulatory compliance, and assist with training and data integrity verification.

The Sr. CRA II will oversee study site monitoring, ensure protocol compliance, manage data integrity, and coordinate clinical projects while traveling frequently.

Responsible for site monitoring, ensuring protocol compliance, data integrity, and training new employees for clinical trials in oncology.

The Sr. CRA 2 is responsible for monitoring clinical trials, ensuring compliance with protocols, managing site activities, and training staff while traveling up to 60%.

Lead and support clinical trials in Ophthalmology, overseeing monitoring and site management while ensuring adherence to protocols and data integrity.